Skip to main content
Clinical Trials/NCT00011609
NCT00011609
Completed
Phase 2

Clinical Evaluation of a Wheelchair Mounted Robotic Arm

US Department of Veterans Affairs1 site in 1 country30 target enrollmentAugust 2000

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Spinal Cord Injury
Sponsor
US Department of Veterans Affairs
Enrollment
30
Locations
1
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The primary purpose of this project, is to evaluate the effect of a wheelchair mounted robotic arm (WMRA) to improve the functional independence of veterans with SCI.

The study will determine if the ability to perform marker tasks within the following four categories is improved after the 4 week training period using the robotic arm:

  1. activities of daily living, 2. vocational tasks, 3. advanced tasks, and subject-specific tasks.

Detailed Description

The primary purpose of this project, is to evaluate the effect of a wheelchair mounted robotic arm (WMRA) to improve the functional independence of veterans with SCI. The study will determine if the ability to perform marker tasks within the following four categories is improved after the 4 week training period using the robotic arm: 1. activities of daily living, 2. vocational tasks, 3. advanced tasks, and subject-specific tasks. The secondary purposes of this project are the following: 1.Does quality of life (life satisfaction and health status) improve after a 4 week period of using the WMRA? 2. What are the perceived advantages of the WMRA to the veteran with SCI? Additionally, the study will evaluate the following: 1) ease of installation and usefulness of instructional manuals; 2) training requirements (time, tasks); 3) safety features; 4) reliability of the device; 5) home, community, and vocational applications; 6) user acceptability; 7) maintenance/ service; 8) portability; and possible modifications.

Registry
clinicaltrials.gov
Start Date
August 2000
End Date
November 2001
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

Loading locations...

Similar Trials